Allele Registry

Canonical Allele Identifier: PA144295

Gene: CUBN HGNC NCBI

ClinVar Allele:

70978

ClinVar RCV:

RCV000049752

ClinVar Variation:

56339

HGVS (amino-acid)	Matching Registered Transcripts
NP_001072.2:p.Gly1390Ser	CA144293 NM_001081.4:c.4168G>A